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Exosome Determinants of Physiological Aging and Age-Related Neurodegenerative Diseases

Aging is consistently reported as the most important independent risk factor for neurodegenerative diseases. As life expectancy has significantly increased during the last decades, neurodegenerative diseases became one of the most critical public health problem in our society. The most investigated...

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Autores principales: D’Anca, Marianna, Fenoglio, Chiara, Serpente, Maria, Arosio, Beatrice, Cesari, Matteo, Scarpini, Elio Angelo, Galimberti, Daniela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6722391/
https://www.ncbi.nlm.nih.gov/pubmed/31555123
http://dx.doi.org/10.3389/fnagi.2019.00232
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author D’Anca, Marianna
Fenoglio, Chiara
Serpente, Maria
Arosio, Beatrice
Cesari, Matteo
Scarpini, Elio Angelo
Galimberti, Daniela
author_facet D’Anca, Marianna
Fenoglio, Chiara
Serpente, Maria
Arosio, Beatrice
Cesari, Matteo
Scarpini, Elio Angelo
Galimberti, Daniela
author_sort D’Anca, Marianna
collection PubMed
description Aging is consistently reported as the most important independent risk factor for neurodegenerative diseases. As life expectancy has significantly increased during the last decades, neurodegenerative diseases became one of the most critical public health problem in our society. The most investigated neurodegenerative diseases during aging are Alzheimer disease (AD), Frontotemporal Dementia (FTD) and Parkinson disease (PD). The search for biomarkers has been focused so far on cerebrospinal fluid (CSF) and blood. Recently, exosomes emerged as novel biological source with increasing interest for age-related neurodegenerative disease biomarkers. Exosomes are tiny Extracellular vesicles (EVs; 30–100 nm in size) released by all cell types which originate from the endosomal compartment. They constitute important vesicles for the release and transfer of multiple (signaling, toxic, and regulatory) molecules among cells. Initially considered with merely waste disposal function, instead exosomes have been recently recognized as fundamental mediators of intercellular communication. They can move from the site of release by diffusion and be retrieved in several body fluids, where they may dynamically reflect pathological changes of cells present in inaccessible sites such as the brain. Multiple evidence has implicated exosomes in age-associated neurodegenerative processes, which lead to cognitive impairment in later life. Critically, consolidated evidence indicates that pathological protein aggregates, including Aβ, tau, and α-synuclein are released from brain cells in association with exosomes. Importantly, exosomes act as vehicles between cells not only of proteins but also of nucleic acids [DNA, mRNA transcripts, miRNA, and non-coding RNAs (ncRNAs)] thus potentially influencing gene expression in target cells. In this framework, exosomes could contribute to elucidate the molecular mechanisms underneath neurodegenerative diseases and could represent a promising source of biomarkers. Despite the involvement of exosomes in age-associated neurodegeneration, the study of exosomes and their genetic cargo in physiological aging and in neurodegenerative diseases is still in its infancy. Here, we review, the current knowledge on protein and ncRNAs cargo of exosomes in normal aging and in age-related neurodegenerative diseases.
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spelling pubmed-67223912019-09-25 Exosome Determinants of Physiological Aging and Age-Related Neurodegenerative Diseases D’Anca, Marianna Fenoglio, Chiara Serpente, Maria Arosio, Beatrice Cesari, Matteo Scarpini, Elio Angelo Galimberti, Daniela Front Aging Neurosci Neuroscience Aging is consistently reported as the most important independent risk factor for neurodegenerative diseases. As life expectancy has significantly increased during the last decades, neurodegenerative diseases became one of the most critical public health problem in our society. The most investigated neurodegenerative diseases during aging are Alzheimer disease (AD), Frontotemporal Dementia (FTD) and Parkinson disease (PD). The search for biomarkers has been focused so far on cerebrospinal fluid (CSF) and blood. Recently, exosomes emerged as novel biological source with increasing interest for age-related neurodegenerative disease biomarkers. Exosomes are tiny Extracellular vesicles (EVs; 30–100 nm in size) released by all cell types which originate from the endosomal compartment. They constitute important vesicles for the release and transfer of multiple (signaling, toxic, and regulatory) molecules among cells. Initially considered with merely waste disposal function, instead exosomes have been recently recognized as fundamental mediators of intercellular communication. They can move from the site of release by diffusion and be retrieved in several body fluids, where they may dynamically reflect pathological changes of cells present in inaccessible sites such as the brain. Multiple evidence has implicated exosomes in age-associated neurodegenerative processes, which lead to cognitive impairment in later life. Critically, consolidated evidence indicates that pathological protein aggregates, including Aβ, tau, and α-synuclein are released from brain cells in association with exosomes. Importantly, exosomes act as vehicles between cells not only of proteins but also of nucleic acids [DNA, mRNA transcripts, miRNA, and non-coding RNAs (ncRNAs)] thus potentially influencing gene expression in target cells. In this framework, exosomes could contribute to elucidate the molecular mechanisms underneath neurodegenerative diseases and could represent a promising source of biomarkers. Despite the involvement of exosomes in age-associated neurodegeneration, the study of exosomes and their genetic cargo in physiological aging and in neurodegenerative diseases is still in its infancy. Here, we review, the current knowledge on protein and ncRNAs cargo of exosomes in normal aging and in age-related neurodegenerative diseases. Frontiers Media S.A. 2019-08-28 /pmc/articles/PMC6722391/ /pubmed/31555123 http://dx.doi.org/10.3389/fnagi.2019.00232 Text en Copyright © 2019 D’Anca, Fenoglio, Serpente, Arosio, Cesari, Scarpini and Galimberti. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
D’Anca, Marianna
Fenoglio, Chiara
Serpente, Maria
Arosio, Beatrice
Cesari, Matteo
Scarpini, Elio Angelo
Galimberti, Daniela
Exosome Determinants of Physiological Aging and Age-Related Neurodegenerative Diseases
title Exosome Determinants of Physiological Aging and Age-Related Neurodegenerative Diseases
title_full Exosome Determinants of Physiological Aging and Age-Related Neurodegenerative Diseases
title_fullStr Exosome Determinants of Physiological Aging and Age-Related Neurodegenerative Diseases
title_full_unstemmed Exosome Determinants of Physiological Aging and Age-Related Neurodegenerative Diseases
title_short Exosome Determinants of Physiological Aging and Age-Related Neurodegenerative Diseases
title_sort exosome determinants of physiological aging and age-related neurodegenerative diseases
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6722391/
https://www.ncbi.nlm.nih.gov/pubmed/31555123
http://dx.doi.org/10.3389/fnagi.2019.00232
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